VEGGIOTTI, PIERANGELO

VEGGIOTTI, PIERANGELO  

Dipartimento di Scienze Biomediche e Cliniche  

Risultati 1 - 20 di 156 (tempo di esecuzione: 0.005 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
19q13.11 cryptic deletion : description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias 1-gen-2012 Veggiotti P + Article (author) -
3D facial morphometry in Italian patients affected by Aicardi syndrome 1-ott-2020 Daniele GibelliClaudia DolciAnnalisa CappellaPierangelo VeggiottiChiarella Sforza + Article (author) -
Abnormal cerebellar functional MRI connectivity in patients with paediatric multiple sclerosis 1-mar-2016 P. Veggiotti + Article (author) -
Acquired epileptic frontal syndrome as long-term outcome in two children with CSWS 1-gen-2001 Veggiotti P + Article (author) -
Acute chorea in a child receiving second dose of human papilloma virus vaccine 1-gen-2014 V. De GiorgisP. Veggiotti + Article (author) -
Acute encephalitis in pediatric multisystem inflammatory syndrome associated with COVID-19 1-gen-2021 Basso E.Lavatelli R.Previtali R.Zuccotti G. V.Veggiotti P. + Article (author) -
Aspetti clinici e molecolari in un paziente pediatrico affetto da Sindrome di Leigh associata alla mutazione mitocondriale m.14459G>A 1-gen-2010 D. RonchiA. BordoniF. FortunatoE. FassoneP. VeggiottiG.P. Comi + Conference Object -
Atypical Manifestations in Glut1 Deficiency Syndrome 1-ago-2016 P. Veggiotti + Article (author) -
Auditory attention at the onset of West syndrome: correlation with EEG patterns and visual function 1-gen-2006 Veggiotti P + Article (author) -
Basal ganglia dysmorphism in patients with Aicardi syndrome 1-gen-2021 Arrigoni, FilippoDe Giorgis, ValentinaLa Briola, FrancescaParisi, PasqualeVignoli, AglaiaVeggiotti, Pierangelo + Article (author) -
Benign convulsions associated with mild gastroenteritis : a multicenter clinical study 1-gen-2011 Veggiotti P + Article (author) -
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 1-mar-2020 Veggiotti P. + Article (author) -
Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case 1-gen-2006 Veggiotti P + Article (author) -
Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet 1-gen-2017 P. Veggiotti + Article (author) -
Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome 1-feb-2017 P. Veggiotti + Article (author) -
Brain macro- and microscopic damage in patients with paediatric MS 1-gen-2010 Veggiotti P + Article (author) -
Case Report: Novel Compound Heterozygous RNASEH2B Mutations Cause Aicardi–Goutières Syndrome 26-apr-2021 Veggiotti, PierangeloZuccotti, Gian Vincenzo + Article (author) -
CDKL5 deficiency disorder in males : Five new variants and review of the literature 30-apr-2021 Veggiotti, Pierangelo + Article (author) -
The changing face of dietary therapy for epilepsy 1-ott-2016 P. Veggiotti + Article (author) -
CHD2 variants are a risk factor for photosensitivity in epilepsy 1-mag-2015 P. Veggiotti + Article (author) -